Prenatal Testing for Duchenne & Becker Muscular Dystrophy
Lancet 1:262-266, Cole,C.G.,et al, 1988
Morphologic Changes in the Muscles of Patients with Postpoliomyelitis Neuromuscular Symptoms
Neurol 38:99-104, Dalakas,M.C., 1988
Neurofibromatosis 2 (Bilateral Acoustic Neuro-fibromatosis)
NEJM 318:684-688, Martuza,R.L.&Eldridge,R., 1988
Local Intra-Arterial Fibrinolytic Therapy in Acute Carotid Territory Stroke, A Pilot Study
Stroke 19:307-313, delZoppo,G.J.,et al, 1988
Thrombolytic Therapy:Current Status (Second of Two Parts)
NEJM 318:1585-1595, Marder,V.J.&Sherry,S., 1988
Intracarotid Urokinase with Thromboembolic Occlusion of the Middle Cerebral Artery
Stroke 19:802-812, Mori,E.,et al, 1988
Presymptomatic Neuropsychological Impairment in Huntington's Disease
Arch Neurol 45:769-773, Jason,G.W.,et al, 1988
Gene Studies in Newborn Males with Duchenne Muscular Dystrophy Detected by Neonatal Screening
Lancet 2:425-427, Greenberg,C.R.,et al, 1988
Functional Recovery, A Major Risk Factor for the Development of Postpoliomyelitis Muscular Atrophy
Arch Neurol 45:645-647, Klingman,J.,et al, 1988
Motoneuron Disease and Past Poliomyelitis in England and Wales
Lancet 1:1319-1322, Martyn,C.N.,et al, 1988
Neurofibromatosis 2:Clinical & DNA Linkage Studies of a Large Kindred
Wertelecki. W. , et al, NEJM 319:276-2838., , 1988
Thrombolytic Therapy in Cerebrovascular Disease
Stroke 19:1174-1179, DelZoppo,G.J., 1988
Mutation in Cystatin C Gene Causes Hereditary Brain Hemorrhage
Lancet 2:603-604, Palsdottir,A.,et al, 1988
Genetic Markers for Neurofibromatosis
Editorial, Lancet 2:719-7201988., , 1988
Intra-arterial Thrombolytic Therapy Improves Outcome in Patients with Acute Vertebrobasilar Occlusive Disease
Stroke 19:1216-1222, Hacke,W.,et al, 1988
Fatal Ischaemic Brain Oedema after Early Thrombolysis with Tissue Plasminogen Activator in Acute Stroke
BMJ 297:1571-1574, Koudstaal,P.J.,et al, 1988
Intracerebral Hemorrhage Complicating Intravenous Tissue Plasminogen Activator Treatment
Arch Neurol 45:1070-1073, Carlson,S.E.,et al, 1988
The Molecular Genetic Revolution, Its Impact on Clinical Neurology
Arch Neurol 45:1366-1376, Payne,C.S.&Roses,A.D., 1988
Use of Ancrod in Acute or Progressing Ischemic Cerebral Infarction
Ann Emerg Med 17:1208-1209, Olinger,C.P.,et al, 1988
Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988
Late Denervation in Patients with Antecedent Paralytic Poliomyelitis
NEJM 317:7-12, Cashman,N.R.,et al, 1987
Transplantation in Parkinson's Disease:Two Cases of Adrenal Medullary Grafts to the Putamen
Ann Neurol 22:457-468, Lindvall,O.,et al, 1987
Hereditary Motor & Sensory Neuropathy, X-Linked:A Half Century Follow-Up
Neurol 37:1460-1465, Rozear,M.P.,et al, 1987
Current Medical & Surgical Therapy for Cerebrovascular Disease
NEJM 317:1505-1516, Grotta,J.C., 1987
Effective Strategy for Prenatal Prediction of Duchenne & Becker Muscular Dystrophy
Lancet 2:1294-1296, Forrest,S.M.,et al, 1987
Diaphragm Pacing for Ventilatory Insufficiency
J Inten Care Med 2:345-353, Marcy,T.W.&Loke,J.S., 1987
Genetic Linkage in Neurologic Diseases
Editorial, NEJM 316:1018-10201987., Martin,J.B., 1987
Prenatal Diagnosis & Detection of Carriers with DNA Probes in Duchenne's Muscular Dystrophy
NEJM 316:985-993, 1018-10201987., Darras,B.T.,et al, 1987
Thrombolysis & Stroke, Past & Future
Arch Neurol 44:748-768, Sloan,M.A., 1987
The Combined Use of Positron Emission Tomography & DNA Polymorphisms for Preclinical Detection of Huntington's Disease
Neurol 37:1441-1447, Hayden,M.R.,et al, 1987
First-Trimester Prenatal Diagnosis for Huntington's Disease with DNA Probes
et al Lancet 1:1284-1285, Hayden,M.R., 1987
Alzheimer's Disease
Down's Syndrome, & Chromosome 21, Editorial, Lancet 1:1011-1012., , 1987
Neurologic Complications in Oral Polio Vaccine Recipients
J Pediatr 108:878-881, Gaebler,J.W., 1986
Location of the Gene for X-Linked Spinal Muscular Atrophy
Neurol 36:1595-1598, Fischbeck,K.H.,et al, 1986
Late Sequelae of Poliomyelitis
Editorial, Lancet 2:1195-11961986., , 1986
Neonatal Paralytic Poliomyelitis
Arch Neurol 43:192-194, Bergeisen,G.H.,et al, 1986
A Long-Term Follow-Up Study of Patients with Post-Poliomyelitis Neuromuscular Symptoms
NEJM 314:959-963, Dalakas,M.C.,et al, 1986
Huntington's Disease, Pathogenesis & Management
NEJM 315:1267-1276, Martin,J.B.&Gusella,J.F., 1986
Classification of Peripheral Neuropathy:The Long and the Short of It
Muscle & Nerve 9:711-719986., Sabin,T.J., 1986
Post-Polio Syndrome
J Med Assoc Ga 74:510-511, Bailey,A.A., 1985
Genetic Prediction & Family Structure in Huntington's Chorea
BMJ 290:1929-1931, Harper,P.S.,et al, 1985
Prenatal Diagnosis & Carrier Detection of Duchenne Muscular Dystrophy with Closely Linked RFLPs
Lancet 1:655-658, Bakker,E.,et al, 1985
Cerebrovascular Complications of Streptokinase Infusion
JAMA 253:1777-1779, Aldrich,M.S.,et al, 1985
A DNA Polymorphism for Huntington's Disease Marks the Future
Arch Neurol 42:20-24, Wexler,N.S.,et al, 1985
Genetic Testing in Huntington's Disease
Ann Neurol 16:511-513, Koller,W.C.,et al, 1984
Sudden Infant Death Syndrome Caused by Poliomyelitis
Arch Neurol 41:775-777, Dunne,J.W.,et al, 1984
Molecular Genetics, Recombinant DNA Techniques, & Genetic Neurological Disease
Ann Neurol 15:511-520, Rosenberg,R.N., 1984
Controlled Trial of Ancrod in Ischemic Stroke
Arch Neurol 40:803-808, Hossman,V.,et al, 1983
Recombinant DNA & Neurologic Disease:The Coming of a New Age
Neurol 33:622-625, Rosenberg,R.N., 1983
A Genetic Marker for Huntington's Chorea
BMJ 287:1567-1568, Harper,P.S., 1983